FDA recall record

Beaver Visitec International CustomEyes kits recall — FDA Z-1200-2023

Device packaging may contain open seals, compromising product sterility.

Class IIclassification
Z-1200-2023official record ID
Mar 8, 2023report date

Recall record at a glance

Official recordZ-1200-2023
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmBeaver Visitec International, Inc.
Report dateMar 8, 2023
Recall initiation dateDec 20, 2022
Quantity4640 units in total
LocationWaltham, MA, United States

Official product description

CustomEyes kits

Why the product was recalled

Device packaging may contain open seals, compromising product sterility.

Distribution information

US distribution in AL, CA, CO, DC, FL, GA, IL, LA, MD, MN, MT, NC, NH, NJ, NM, NY, OH OK, PA, RI, TN, TX, UT, VA, VT, WA, and WI OUS distribution to Canada, Japan, and South Africa

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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